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£¨3£©2H2S(g) + 3O2(g) ?2SO2(g) + 2H2O(l) ½â£º
ϰÌâ2-14 Calculate the standard molar enthalpy of formation for N2O5(g) from the following date:
£¨1£©2NO(g) + O2(g) ?2NO2(g) £¨2£©4NO2(g) + O2(g) ?2N2O5(g) £¨3£©N2(g) + O2(g) ?2NO(g)
¦È(3) = -180.5kJ¡¤ ?rHmmol-1
¦È¦È¦È¦È¦È
¦Èmol-1 ?rHm(1) = -114.1 kJ¡¤
¦È(2= -110.2kJ¡¤ ?rHmmol-1
½â£º 0.5?(2)+£¨1)+(3)µÃ(4£© N2(g) + 2.5O2(g) ? N2O5(g)
ϰÌâ2-15 A sample of D-ribose (C5H10O5) with mass 0.727g was weighed into a calorimeter and then ignited in presence of excess Oxygen. The temperature rose by 0.910K when the sample was
combusted. In a separate experiment in the same calorimeter the combustion of 0.825g of benzoic
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?acid(C7H6O2), for which the ¦¤cUm?3251kJ?mol?1, gave a temperature rise of 1.940K. Calculate the
¦È¦È?rUm and ?rHm of D-ribose combusted.
½â£º 0.825g±½¼×ËáȼÉÕ£¬ÒÇÆ÷ζÈÉÏÉý1.940K, ÉèË®µ±Á¿£¨ÒÇÆ÷ζÈÉÏÉý1KËùÐèµÄÈÈÁ¿£©ÎªQ,
= 11.33?103J?K-1
0.727g D-ºËËáȼÉÕ£¬ÒÇÆ÷ζÈÉÏÉý0.910K£¬
C5H10O5(s) + 5O2 (g) ? 5CO2(g) + 5H2O(l)
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